首页> 外文期刊>Journal of Medicinal Chemistry >Potent Antitumor Activities and Structure Basis of the Chiral beta-Lactam Bridged Analogue of Combretastatin A-4 Binding to Tubulin
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Potent Antitumor Activities and Structure Basis of the Chiral beta-Lactam Bridged Analogue of Combretastatin A-4 Binding to Tubulin

机译:Combretastatin A-4与微管蛋白结合的手性β-内酰胺桥接类似物的强抗肿瘤活性和结构基础。

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摘要

A series of chiral,beta-lactam bridged analogues (3-substituted 1,4-diaryl-2-azetidinones) of combretastatin A-4 (CA-4) were synthesized asymmetrically, and their antitumor activities were evaluated in vitro and in vivo. The cocrystal structure of tubulin in complex with compound 9 was determined by X-ray crystallography, which showed that 9 binds to the same site as colchicine with similar binding mode, and the absolute configuration of its C-4 was first identified and demonstrated to be critically important for their antiproliferative activities.
机译:不对称地合成了康布雷他汀A-4(CA-4)的一系列手性,β-内酰胺桥连的类似物(3-取代的1,4-二芳基-2-氮杂环丁酮),并在体内和体外评估了它们的抗肿瘤活性。 X射线晶体学测定微管蛋白与化合物9的复合物的共晶体结构,结果表明9与秋水仙碱以相同的结合方式结合在同一位点上,并首次鉴定出其C-4的绝对构型为对它们的抗增殖活性至关重要。

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